TY - JOUR
T1 - Declining fecundity and ovarian ageing in natural fertility populations
AU - O'Connor, Kathleen A.
AU - Holman, Darryl J.
AU - Wood, James W.
N1 - Funding Information:
We thank the following organizations for their support of the research discussed in this paper: the National Institute on Aging (NIA 1 RO1 AG15141-01; 5 T32 AG00208), the National Institute of Child Health and Human Development (NICHD 1 HD 28263-01; F32 HD 07994-02; 2 P30 HD28263-05); the National Science Foundation (DBS-9218734), and the Population Council. Research in Bangladesh was supported by a Dissertation Research Grant on International Demographic Issues made on behalf of the Andrew W. Mellon Foundation to the Population Research Institute, the Hill Foundation, the American Institute of Bangladesh Studies, the Centre for Development Research, Bangladesh, and the International Centre for Diarrhoeal Disease Research, Bangladesh. For laboratory assistance, we thank Eleanor Brindle and Susannah Barsom. For assistance with assay development and antibodies we are grateful to John O'Connor, Fortune Kohen, Bill Lasley, Ken Campbell and Cheryl Stroud. Anti-human LHβ1 and FSHβ antisera (AFP #1) and LH (AFP4261A) and FSH (LER907) standards were provided by the National Hormone and Pituitary Program through NIDDK, NICHD, and USDA. Finally, we are grateful to Ares-Serono, Abbott, and Dr Egbert te Velde for sponsoring and organizing the workshop on Ovarian Ageing.
PY - 1998/10/12
Y1 - 1998/10/12
N2 - Worldwide, human fertility declines with increasing maternal age, after contraceptive-use patterns and behavioral factors are taken into consideration. Here, we summarize some of our theoretical and empirical work examining the biological factors contributing to this age pattern of fertility. We undertook an 11 month prospective endocrinological study in a natural fertility (non-contracepting) population (rural Bangladesh) to estimate the contributions of fetal loss and fecundability (the probability of conception) to declining fecundity with age. Prospective interviews and urine samples for pregnancy tests were collected twice weekly from up to 700 women. These data were used to test mathematical models of the underlying biological processes contributing to changing fecundability and fetal loss risk with maternal age. The results indicate that much of the decline in fecundity can be attributed to an increasing risk of fetal loss with maternal age. Much of this fetal loss is due to chromosomal abnormalities-a result of ageing oocytes. Fecundability, on the other hand, does not begin to decline until the early 40s. We hypothesize that this is also a result of ageing at the ovarian level, namely follicular atresia, in the years just prior to menopause. The irregularity of menstrual cycles-longer cycles and increasingly variable hormonal patterns-at these ages may be a direct result of the small and rapidly dwindling remaining pool of follicles. We present a simple mathematical model of this process, and some preliminary laboratory results that support the model. Copyright (C) 1998 Elsevier Science Ireland Ltd.
AB - Worldwide, human fertility declines with increasing maternal age, after contraceptive-use patterns and behavioral factors are taken into consideration. Here, we summarize some of our theoretical and empirical work examining the biological factors contributing to this age pattern of fertility. We undertook an 11 month prospective endocrinological study in a natural fertility (non-contracepting) population (rural Bangladesh) to estimate the contributions of fetal loss and fecundability (the probability of conception) to declining fecundity with age. Prospective interviews and urine samples for pregnancy tests were collected twice weekly from up to 700 women. These data were used to test mathematical models of the underlying biological processes contributing to changing fecundability and fetal loss risk with maternal age. The results indicate that much of the decline in fecundity can be attributed to an increasing risk of fetal loss with maternal age. Much of this fetal loss is due to chromosomal abnormalities-a result of ageing oocytes. Fecundability, on the other hand, does not begin to decline until the early 40s. We hypothesize that this is also a result of ageing at the ovarian level, namely follicular atresia, in the years just prior to menopause. The irregularity of menstrual cycles-longer cycles and increasingly variable hormonal patterns-at these ages may be a direct result of the small and rapidly dwindling remaining pool of follicles. We present a simple mathematical model of this process, and some preliminary laboratory results that support the model. Copyright (C) 1998 Elsevier Science Ireland Ltd.
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U2 - 10.1016/S0378-5122(98)00068-1
DO - 10.1016/S0378-5122(98)00068-1
M3 - Article
C2 - 9871907
AN - SCOPUS:0031722063
SN - 0378-5122
VL - 30
SP - 127
EP - 136
JO - Maturitas
JF - Maturitas
IS - 2
ER -